Philips Senior Supplier Quality Engineer 

United States, Minnesota 

77756072

Senior Supplier Quality Engineer

In this role you

Improve sourcing support of our New Product Development (NPD) function by developing and leading robust sourcing processes that drive selection of the best suppliers based on all technical, quality and business (including cost) requirements throughout the product lifecycle.

Your role:

• Proactively manage, monitor, and troubleshoot supplier-related issues for quality of components, sub-assemblies, and assemblies including monitoring trends and managingSupplier Improvement and Supplier Quality Performance Monitoring.
• Providing Quality oversight of product/process change requests from suppliers, ensuring appropriate regulatory review and adequate validation to support requested changes including following our APQP process and leading process validation, as necessary.
• Act as a technical liaison between Philips and suppliers for Sustaining Engineering. Collaborate with suppliers in defining supplied material specifications, identifying critical component features and supplier manufacturing processes, developing and validating supplier manufacturing processes, and implementing appropriate process controls and monitoring
• Assuring technical quality of suppliers, manufacturers, and OEMs is maintained and acceptance criteria are in alignment with component/product use and customer expectations.
• Support supplier selection, classification, approval, and development through a combination ofassessing supplier technical capabilities, supplier quality controls, adherence to design controls, audit, and inspection experience.

You're the right fit if:

• BS in Mechanical, Electrical, Biomedical, or Industrial Engineering, or related technical discipline preferred
• 5+ years of Supplier Quality Engineering experience in a medical device (Class II & III) or similar environment with manufacturing or product quality as a focus.
• Your skills include the ability to demonstrate technical innovation, technical leadership, mechanical and/or electrical engineering, understanding of and adherence to GMP practices and FDA regulations and the knowledge and use of relevant PC software applications, including statistical software, and skills to use them effectively.
• You have strong interactive skills in general communication, cross-functional participation and influence, mentoring and acceptance of guidance, technical leadership, project management, coordination with cross-functional team member, team behavior, and support for subordinates, junior engineers, technicians, and management.
• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.

How we work together

This is an office role.

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

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The pay range for this position in Plymouth MN is $93,000 to $131,000, Annually.

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US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

within commuting distance to Plymouth MN.